Cuscuta Spp.) in Ornamental Crop Production and Landscapes1 Kaley Mierek, Chris Marble, Nathan Boyd, and Shawn Steed2
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The Evolution of Sexual Reproduction in Cuscuta (Convolvulaceae)
Wilfrid Laurier University Scholars Commons @ Laurier Theses and Dissertations (Comprehensive) 2011 The Evolution of Sexual Reproduction in Cuscuta (Convolvulaceae) Michael Wright Wilfrid Laurier University Follow this and additional works at: https://scholars.wlu.ca/etd Part of the Plant Breeding and Genetics Commons Recommended Citation Wright, Michael, "The Evolution of Sexual Reproduction in Cuscuta (Convolvulaceae)" (2011). Theses and Dissertations (Comprehensive). 1039. https://scholars.wlu.ca/etd/1039 This Thesis is brought to you for free and open access by Scholars Commons @ Laurier. It has been accepted for inclusion in Theses and Dissertations (Comprehensive) by an authorized administrator of Scholars Commons @ Laurier. For more information, please contact [email protected]. NOTE TO USERS This reproduction is the best copy available. UMI Library and Archives Bibliotheque et 1*1 Canada Archives Canada Published Heritage Direction du Branch Patrimoine de I'edition 395 Wellington Street 395, rue Wellington OttawaONK1A0N4 OttawaONK1A0N4 Canada Canada Your file Votre reference ISBN: 978-0-494-75396-5 Our file Notre reference ISBN: 978-0-494-75396-5 NOTICE: AVIS: The author has granted a non L'auteur a accorde une licence non exclusive exclusive license allowing Library and permettant a la Bibliotheque et Archives Archives Canada to reproduce, Canada de reproduire, publier, archiver, publish, archive, preserve, conserve, sauvegarder, conserver, transmettre au public communicate to the public by par telecommunication ou par I'lnternet, preter, telecommunication or on the Internet, distribuer et vendre des theses partout dans le loan, distribute and sell theses monde, a des fins commerciaies ou autres, sur worldwide, for commercial or non support microforme, papier, electronique et/ou commercial purposes, in microform, autres formats. -
Horner-Mclaughlin Woods Compiled by Bev Walters, 2011-2012
Horner-McLaughlin Woods Compiled by Bev Walters, 2011-2012 SCIENTIFIC NAME COMMON NAME Acer negundo BOX-ELDER Acer nigrum (A. saccharum) BLACK MAPLE Acer rubrum RED MAPLE Acer saccharinum SILVER MAPLE Acer saccharum SUGAR MAPLE Achillea millefolium YARROW Actaea pachypoda DOLL'S-EYES Adiantum pedatum MAIDENHAIR FERN Agrimonia gryposepala TALL AGRIMONY Agrimonia parviflora SWAMP AGRIMONY Agrimonia pubescens SOFT AGRIMONY AGROSTIS GIGANTEA REDTOP Agrostis perennans AUTUMN BENT Alisma subcordatum (A. plantago-aquatica) SOUTHERN WATER-PLANTAIN Alisma triviale (A. plantago-aquatica) NORTHERN WATER-PLANTAIN ALLIARIA PETIOLATA GARLIC MUSTARD Allium tricoccum WILD LEEK Ambrosia artemisiifolia COMMON RAGWEED Amelanchier arborea JUNEBERRY Amelanchier interior SERVICEBERRY Amphicarpaea bracteata HOG-PEANUT Anemone quinquefolia WOOD ANEMONE Anemone virginiana THIMBLEWEED Antennaria parlinii SMOOTH PUSSYTOES Apocynum androsaemifolium SPREADING DOGBANE ARCTIUM MINUS COMMON BURDOCK Arisaema triphyllum JACK-IN-THE-PULPIT Asarum canadense WILD-GINGER Asclepias exaltata POKE MILKWEED Asclepias incarnata SWAMP MILKWEED Asplenium platyneuron EBONY SPLEENWORT Athyrium filix-femina LADY FERN BERBERIS THUNBERGII JAPANESE BARBERRY Bidens cernua NODDING BEGGAR-TICKS Bidens comosa SWAMP TICKSEED Bidens connata PURPLE-STEMMED TICKSEED Bidens discoidea SWAMP BEGGAR-TICKS Bidens frondosa COMMON BEGGAR-TICKS Boehmeria cylindrica FALSE NETTLE Botrypus virginianus RATTLESNAKE FERN BROMUS INERMIS SMOOTH BROME Bromus pubescens CANADA BROME Calamagrostis canadensis BLUE-JOINT -
Cassytha Pubescens
Cassytha pubescens: Germination biology and interactions with native and introduced hosts Hong Tai (Steven), Tsang B.Sc. Hons (University of Adelaide) Thesis submitted for the degree of Master of Science School of Earth & Environmental Science University of Adelaide, Australia 03/05/2010 i Table of Contents Table of Contents ........................................................................................................... ii Abstract .......................................................................................................................... v Declaration ................................................................................................................... vii Acknowledgements .................................................................................................... viii Chapter. 1 Introduction .................................................................................................. 1 1.1 General Introduction ............................................................................................ 1 1.2 Literature Review ................................................................................................. 3 1.2.1 Characteristics of parasitic control agents .................................................... 3 1.2.2. Direct impacts on hosts ................................................................................ 7 1.2.3. Indirect impacts on hosts ............................................................................. 8 1.2.4. Summary ................................................................................................... -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
Convolvulaceae1
Photograph: Helen Owens © Department of Environment, Water and Natural Resources, Government of South Australia Department of All rights reserved Environment, Copyright of illustrations might reside with other institutions or Water and individuals. Please enquire for details. Natural Resources Contact: Dr Jürgen Kellermann Editor, Flora of South Australia (ed. 5) State Herbarium of South Australia PO Box 2732 Kent Town SA 5071 Australia email: [email protected] Flora of South Australia 5th Edition | Edited by Jürgen Kellermann CONVOLVULACEAE1 R.W. Johnson2 Annual or perennial herbs or shrubs, often with trailing or twining stems, or leafless parasites; leaves alternate, exstipulate. Inflorescence axillary, rarely terminal, cymose or reduced to a single flower; flowers regular, (4) 5 (6)-merous, bisexual; sepals free or rarely united, quincuncial; corolla sympetalous, funnel-shaped or campanulate, occasionally rotate or salver-shaped; stamens adnate to the base of the corolla, alternating with the corolla lobes, filaments usually flattened and dilated downwards; anthers 2-celled, dehiscing longitudinally; ovary superior, mostly 2-celled, occasionally with 1, 3 or 4 cells, subtended by a disk; ovules 2, rarely 1, in each cell; styles 1 or 2, stigmas variously shaped. Fruit capsular. About 58 genera and 1,650 species mainly tropical and subtropical; in Australia 20 genera, 1 endemic, with c. 160 species, 17 naturalised. The highly modified parasitic species of Cuscuta are sometimes placed in a separate family, the Cuscutaceae. 1. Yellowish leafless parasitic twiners ...................................................................................................................... 5. Cuscuta 1: Green leafy plants 2. Ovary distinctly 2-lobed; styles 2, inserted between the lobes of ovary (gynobasic style); leaves often kidney-shaped ............................................................................................................. -
Cassytha) and Insights Into the Plastid Phylogenomics of Lauraceae
GBE Plastome Evolution in the Sole Hemiparasitic Genus Laurel Dodder (Cassytha) and Insights into the Plastid Phylogenomics of Lauraceae Chung-Shien Wu1,†, Ting-Jen Wang1,†,Chia-WenWu1, Ya-Nan Wang2, and Shu-Miaw Chaw1,* 1Biodiversity Research Center, Academia Sinica, Taipei 11529, Taiwan 2School of Forestry and Resource Conservation, Nation Taiwan University, Taipei 10617, Taiwan *Corresponding author: E-mail: [email protected]. †These authors contributed equally to this work. Accepted: September 6, 2017 Data deposition: This project has been deposited at DDBJ under the accession numbers LC210517, LC212965, LC213014, and LC228240. Abstract To date, little is known about the evolution of plastid genomes (plastomes) in Lauraceae. As one of the top five largest families in tropical forests, the Lauraceae contain many species that are important ecologically and economically. Lauraceous species also provide wonderful materials to study the evolutionary trajectory in response to parasitism because they contain both nonparasitic and parasitic species. This study compared the plastomes of nine Lauraceous species, including the sole hemiparasitic and herbaceous genus Cassytha (laurel dodder; here represented by Cassytha filiformis). We found differential contractions of the canonical inverted repeat (IR), resulting in two IR types present in Lauraceae. These two IR types reinforce Cryptocaryeae and Neocinnamomum— Perseeae–Laureae as two separate clades. Our data reveal several traits unique to Cas. filiformis, including loss of IRs, loss or pseudogenization of 11 ndh and rpl23 genes, richness of repeats, and accelerated rates of nucleotide substitutions in protein- coding genes. Although Cas. filiformis is low in chlorophyll content, our analysis based on dN/dS ratios suggests that both its plastid house-keeping and photosynthetic genes are under strong selective constraints. -
1083 a Ground-Breaking Study Published 5 Years Ago Revealed That
American Journal of Botany 100(6): 1083–1094. 2013. SPECIAL INVITED PAPER—EVOLUTION OF PLANT MATING SYSTEMS P OLLINATION AND MATING SYSTEMS OF APODANTHACEAE AND THE DISTRIBUTION OF REPRODUCTIVE TRAITS 1 IN PARASITIC ANGIOSPERMS S IDONIE B ELLOT 2 AND S USANNE S. RENNER 2 Systematic Botany and Mycology, University of Munich (LMU), Menzinger Str. 67 80638 Munich, Germany • Premise of the study: The most recent reviews of the reproductive biology and sexual systems of parasitic angiosperms were published 17 yr ago and reported that dioecy might be associated with parasitism. We use current knowledge on parasitic lineages and their sister groups, and data on the reproductive biology and sexual systems of Apodanthaceae, to readdress the question of possible trends in the reproductive biology of parasitic angiosperms. • Methods: Fieldwork in Zimbabwe and Iran produced data on the pollinators and sexual morph frequencies in two species of Apodanthaceae. Data on pollinators, dispersers, and sexual systems in parasites and their sister groups were compiled from the literature. • Key results: With the possible exception of some Viscaceae, most of the ca. 4500 parasitic angiosperms are animal-pollinated, and ca. 10% of parasites are dioecious, but the gain and loss of dioecy across angiosperms is too poorly known to infer a statisti- cal correlation. The studied Apodanthaceae are dioecious and pollinated by nectar- or pollen-foraging Calliphoridae and other fl ies. • Conclusions: Sister group comparisons so far do not reveal any reproductive traits that evolved (or were lost) concomitant with a parasitic life style, but the lack of wind pollination suggests that this pollen vector may be maladaptive in parasites, perhaps because of host foliage or fl owers borne close to the ground. -
Larvicide of Aedes Aegypti (Diptera: Culicidae) from Ipomoea Pes-Caprae (Solanales: Convolvulaceae) Musri Musman, Sofyatuddin Karina, Said Almukhsin
AACL BIOFLUX Aquaculture, Aquarium, Conservation & Legislation International Journal of the Bioflux Society Larvicide of Aedes aegypti (Diptera: Culicidae) from Ipomoea pes-caprae (Solanales: Convolvulaceae) Musri Musman, Sofyatuddin Karina, Said Almukhsin Department of Marine Science, Marine and Fisheries Coordinatorate, Syiah Kuala University, Darussalam-Banda Aceh, Indonesia. Corresponding author: M. Musman, [email protected] Abstract. This research aimed to evaluate larvicidal candidate of the extracts of whole parts (roots, stems, leaves, flowers, and seeds) of Ipomoea pes-caprae (L.) R. Br. on Aedes aegypti (Linnaeus, 1762) larvae. The criteria applied to select larvicidal candidate were (1) the concentration of the extract solution must be ≤ 50 ppm, and (2) the larval mortality due to administration of the extract should be reached ≥ 75%. The I. pes-caprae parts were extracted with methanol and water solvents. Refer to the criteria, the methanol extract of the I. pes-caprae leaf was selected as the larvicidal candidate of the A. aegypti larvae. The 3rd instar of A. aegypti larvae was tested with five kinds of concentration of an aqueous solution of I. pes-caprae leaf extracts by completely random design with four replications. The methanol extract of I. pes-caprae leaf showed a very strong larvicide (LC50 was 12.60 ppm) of A. aegypti larvae. Key Words: larvae, Aedes aegypti, Ipomoea pes-caprae, instar, larvicidal candidate, methanol extract. Introduction. Dengue Hemorrhagic Fever (DHF) is a disease spread by the Aedes aegypti (Linnaeus, 1762) mosquito with a rapid rate of transmission and occurs in tropical regions, subtropical, and temperate in the whole world. DHF is one health problem in the world which the number of sufferers have been gradually increasing in quantity (Rao et al 2011). -
Study of Cuscuta Reflexa Roxb. with Reference to Host Diversity, Anatomy and Biochemistry
Available online a t www.scholarsresearch library.com Scholars Research Library Central European Journal of Experimental Biology , 2014, 3 (2):6-12 (http://scholarsresearchlibrary.com/archive.html) ISSN: 2278–7364 Study of Cuscuta reflexa Roxb. with reference to host diversity, anatomy and biochemistry Sandip S. Nikam, Santosh B. Pawar and M. B. Kanade Post Graduate Research Center, Department of Botany, Tuljaram Chaturchand College, Baramati, Dist. Pune, Maharashtra, India _____________________________________________________________________________________________ ABSTRACT Surveys were conducted to find out the host plants of Cuscuta reflexa Roxb. from different localities of Baramati area of Pune District of Maharashtra, India. Host plants were examined for anatomical and biochemical studies. In a survey 29 species, representing 23 genera belong to 15 families were recorded as host plants of Cuscuta. Cuscuta haustorium penetration in host stem and size of the haustorium was specific to host and Cuscuta species. Each transverse section of host stem shows Cuscuta haustorium reached up to the secondary xylem. Polyphenol oxidase activity studied in healthy and infected stem of Bougainvilliea spectabilis, Ficus glomerata, Vitex negundo, Santalum album and Acalypha hispida. The common trend of enzyme activity is stimulatory in infected host plants. Protein content studied in healthy and infected host plants of Bougainvilliea spectabilis, Ficus glomerata, Vitex negundo, Santalum album and Acalypha hispida by C. reflexa Roxb. It is interesting to note that the protein content is markedly stimulated in all infected host plants. The maximum stimulation occurs in Bougainvilliea spectabilis, Vitex negundo, Santalum album and Acalypha hispida compared to Ficus glomerata. Key words : Cuscuta and host plants, anatomy, polyphenol oxidase, protein _____________________________________________________________________________________________ INTRODUCTION Cuscuta (Family - Convolvulaceae) is an obligate angiosperm parasitic climber found commonly throughout India. -
Invisible Connections: Introduction to Parasitic Plants Dr
Invisible Connections: Introduction to Parasitic Plants Dr. Vanessa Beauchamp Towson University What is a parasite? • An organism that lives in or on an organism of another species (its host) and benefits by deriving nutrients at the other's expense. Symbiosis https://www.superpharmacy.com.au/blog/parasites-protozoa-worms-ectoparasites Food acquisition in plants: Autotrophy Heterotrophs (“different feeding”) • True parasites: obtain carbon compounds from host plants through haustoria. • Myco-heterotrophs: obtain carbon compounds from host plants via Image Credit: Flickr User wackybadger, via CC mycorrhizal fungal connection. • Carnivorous plants (not parasitic): obtain nutrients (phosphorus, https://commons.wikimedia.org/wiki/File:Pin nitrogen) from trapped insects. k_indian_pipes.jpg http://www.welivealot.com/venus-flytrap- facts-for-kids/ Parasite vs. Epiphyte https://chatham.ces.ncsu.edu/2014/12/does-mistletoe-harm-trees-2/ By © Hans Hillewaert /, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=6289695 True Parasitic Plants • Gains all or part of its nutrition from another plant (the host). • Does not contribute to the benefit of the host and, in some cases, causing extreme damage to the host. • Specialized peg-like root (haustorium) to penetrate host plants. https://www.britannica.com/plant/parasitic-plant https://chatham.ces.ncsu.edu/2014/12/does-mistletoe-harm-trees-2/ Diversity of parasitic plants Eudicots • Parasitism has evolved independently at least 12 times within the plant kingdom. • Approximately 4,500 parasitic species in Monocots 28 families. • Found in eudicots and basal angiosperms • 1% of the dicot angiosperm species • No monocot angiosperm species Basal angiosperms Annu. Rev. Plant Biol. 2016.67:643-667 True Parasitic Plants https://www.alamy.com/parasitic-dodder-plant-cuscuta-showing-penetration-parasitic-haustor The defining structural feature of a parasitic plant is the haustorium. -
Classification of Convolvulaceae: a Phylogenetic Approach
Systematic Botany (2003), 28(4): pp. 791±806 q Copyright 2003 by the American Society of Plant Taxonomists Classi®cation of Convolvulaceae: A Phylogenetic Approach SASÏA STEFANOVICÂ ,1,3 DANIEL F. A USTIN,2 and RICHARD G. OLMSTEAD1 1Department of Botany, University of Washington, Box 355325, Seattle, Washington 98195-5325; 2Conservation and Science Department, Sonora Desert Museum, 2021 N Kinney Road, Tucson, Arizona 85743; 3Author for correspondence, present address: Department of Biology, Indiana University, 1001 E. Third Street, Bloomington, Indiana, 47405 ([email protected]) Communicating Editor: Paul S. Manos ABSTRACT. Because recent molecular studies, based on multiple data sets from all three plant genomes, have indicated mutually congruent, well-resolved, and well-supported relationships within Convolvulaceae (the morning-glory family), a formal reclassi®cation of this family is presented here. Convolvulaceae, a large family of worldwide distribution, exhibiting a rich diversity of morphological characteristics and ecological habitats, are now circumscribed within twelve tribes. A key to these tribes of Convolvulaceae is offered. The group of spiny-pollen bearing Convolvulaceae (forming ``Echinoconiae'') and tribe Cuscuteae are retained essentially in their traditional sense, Cresseae are circumscribed with only minor modi®- cations, Convolvuleae and Erycibeae are recognized in a restricted sense, while Dichondreae and Maripeae are expanded. Also, to produce a tribal taxonomy that better re¯ects phylogenetic relationships, the concept of Poraneae is abandoned as arti®cial, three new tribes are recognized (Aniseieae, Cardiochlamyeae, and Jacquemontieae), and a new tribal status is proposed for the Malagasy endemic Humbertia (Humbertieae). ``Merremieae'' are tentatively retained even though the mono- phyly of this tribe is not certain.